BCORL1

BCL6 corepressor like 1

Summary

The protein encoded by this gene is a transcriptional corepressor that is found tethered to promoter regions by DNA-binding proteins. The encoded protein can interact with several different class II histone deacetylases to repress transcription. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2010]

Known Variants265 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs180956060	X:129,114,784	G/A	regulatory region variant	—
rs146852038	X:129,118,809	G/C	—	—
rs1928393361	X:129,139,233	G/A	—	uncertain significance
rs1325772447	X:129,139,235	G/A	—	uncertain significance
rs1928395845	X:129,139,244	A/G	—	uncertain significance
rs778701486	X:129,139,269	G/A	—	likely benign
rs1928397980	X:129,139,271	A/C	—	uncertain significance
rs1603105985	X:129,146,562	C/T	—	likely pathogenic
rs2522637904	X:129,146,564	C/G	—	uncertain significance
rs2124436524	X:129,146,570	G/A	—	uncertain significance
rs1179687241	X:129,146,631	G/A	—	uncertain significance
rs1225460628	X:129,146,936	C/T	—	uncertain significance
rs370194529	X:129,146,945	G/A	—	uncertain significance
rs973864978	X:129,146,948	G/C	—	uncertain significance
rs141901231	X:129,146,962	C/T	—	likely benign
rs756903033	X:129,146,978	A/T	—	uncertain significance
rs139887979	X:129,147,028	G/A	—	likely benign
rs2124438652	X:129,147,032	C/T	—	uncertain significance
rs149417325	X:129,147,049	T/C	—	uncertain significance
rs766447653	X:129,147,060	C/T	—	likely benign
rs200478600	X:129,147,061	G/A	—	uncertain significance
rs1172667160	X:129,147,089	C/A	—	uncertain significance
rs41299086	X:129,147,108	C/T	—	benign
rs755647755	X:129,147,135	C/T	—	likely benign
rs1929111309	X:129,147,177	A/T	—	likely benign
rs1189143389	X:129,147,206	A/T	—	uncertain significance
rs376946512	X:129,147,220	G/A	—	likely benign
rs2522646977	X:129,147,250	G/T	—	uncertain significance
rs2124439839	X:129,147,256	G/A	—	uncertain significance
rs36043572	X:129,147,264	T/C	—	likely benign
rs778220343	X:129,147,280	A/G	—	uncertain significance
rs2522647523	X:129,147,304	G/A	—	uncertain significance
rs142564302	X:129,147,339	T/C	—	likely benign
rs1131691335	X:129,147,353	C/G	—	uncertain significance
rs150969957	X:129,147,364	C/T	—	uncertain significance
rs5932715	X:129,147,373	G/A	—	benign
rs267606346	X:129,147,377	C/T	—	uncertain significance
rs1929139326	X:129,147,391	C/T	—	uncertain significance
rs1929145977	X:129,147,445	C/T	—	uncertain significance
rs2522650006	X:129,147,460	C/T	—	uncertain significance
rs143414966	X:129,147,530	C/T	—	uncertain significance
rs61752973	X:129,147,531	G/A	—	benign
rs752320467	X:129,147,532	C/T	—	uncertain significance
rs781562011	X:129,147,548	C/T	—	uncertain significance
rs770800501	X:129,147,585	C/T	—	likely benign
rs1293025980	X:129,147,613	G/T	—	uncertain significance
rs776615469	X:129,147,619	C/G	—	uncertain significance
rs965080918	X:129,147,626	G/T	—	uncertain significance
rs200510623	X:129,147,630	G/A	—	likely benign
rs752016473	X:129,147,642	G/A	—	likely benign
rs1257942270	X:129,147,650	C/G	—	uncertain significance
rs750864364	X:129,147,660	G/A	—	likely benign
rs1177045353	X:129,147,682	C/T	—	uncertain significance
rs373673739	X:129,147,733	G/C	—	uncertain significance
rs1308482747	X:129,147,755	C/A	—	uncertain significance
rs1929180944	X:129,147,803	C/G	—	uncertain significance
rs372535982	X:129,147,807	G/A	—	likely benign
rs2522655490	X:129,147,813	G/A	—	likely benign
rs747692788	X:129,147,840	C/T	—	likely benign
rs768067473	X:129,147,878	C/A	—	likely benign
rs1253901089	X:129,147,880	C/T	—	uncertain significance
rs1166568453	X:129,147,889	G/A	—	uncertain significance
rs752889685	X:129,147,928	C/T	—	uncertain significance
rs2124443763	X:129,147,959	C/G	—	uncertain significance
rs1929205587	X:129,147,995	G/A	—	uncertain significance
rs1165081980	X:129,148,006	G/A	—	uncertain significance
rs1929209697	X:129,148,036	A/G	—	uncertain significance
rs1218505420	X:129,148,096	G/T	—	uncertain significance
rs2124444625	X:129,148,134	T/A	—	uncertain significance
rs2522661578	X:129,148,186	G/A	—	uncertain significance
rs112032085	X:129,148,194	G/A	—	benign
rs1057521638	X:129,148,235	C/T	—	uncertain significance
rs1057523534	X:129,148,243	C/T	—	uncertain significance
rs1929229770	X:129,148,256	C/T	—	uncertain significance
rs771396923	X:129,148,259	A/G	—	uncertain significance
rs190993389	X:129,148,345	G/T	—	uncertain significance
rs1324174941	X:129,148,374	T/C	—	likely benign
rs113450274	X:129,148,407	T/C	—	benign
rs1307555930	X:129,148,436	C/T	—	uncertain significance
rs35616836	X:129,148,447	C/T	—	benign
rs2124447114	X:129,148,504	G/A	—	uncertain significance
rs749559990	X:129,148,510	G/C	—	uncertain significance
rs774393845	X:129,148,520	C/G	—	uncertain significance
rs2522666808	X:129,148,537	A/G	—	uncertain significance
rs199780684	X:129,148,539	C/G	—	likely benign
rs2522667204	X:129,148,573	C/T	—	uncertain significance
rs2522667285	X:129,148,579	A/G	—	uncertain significance
rs2522667324	X:129,148,581	G/A	—	uncertain significance
rs2124447684	X:129,148,606	A/T	—	uncertain significance
rs143864671	X:129,148,637	G/C	—	uncertain significance
rs1603112868	X:129,148,650	A/G	—	likely benign
rs192966850	X:129,148,656	G/A	—	likely benign
rs2522668571	X:129,148,691	C/T	—	uncertain significance
rs148645627	X:129,148,695	C/T	—	likely benign
rs2124448203	X:129,148,735	T/G	—	uncertain significance
rs370391548	X:129,148,764	C/T	—	likely benign
rs1433370540	X:129,148,766	G/T	—	uncertain significance
rs143241923	X:129,148,773	T/A	—	uncertain significance
rs1376395740	X:129,148,795	A/G	—	uncertain significance
rs146730788	X:129,148,803	G/A	—	likely benign

Showing 100 of 265 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.